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The Ca(2+) Sensor Protein Swiprosin-1/EFhd2 Is Present in Neurites and Involved in Kinesin-Mediated Transport in Neurons

Swiprosin-1/EFhd2 (EFhd2) is a cytoskeletal Ca(2+) sensor protein strongly expressed in the brain. It has been shown to interact with mutant tau, which can promote neurodegeneration, but nothing is known about the physiological function of EFhd2 in the nervous system. To elucidate this question, we...

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Detalles Bibliográficos
Autores principales: Purohit, Pavitra, Perez-Branguli, Francesc, Prots, Iryna, Borger, Eva, Gunn-Moore, Frank, Welzel, Oliver, Loy, Kristina, Wenzel, Eva Maria, Grömer, Teja W., Brachs, Sebastian, Holzer, Max, Buslei, Rolf, Fritsch, Kristin, Regensburger, Martin, Böhm, Konrad J., Winner, Beate, Mielenz, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4136728/
https://www.ncbi.nlm.nih.gov/pubmed/25133820
http://dx.doi.org/10.1371/journal.pone.0103976
Descripción
Sumario:Swiprosin-1/EFhd2 (EFhd2) is a cytoskeletal Ca(2+) sensor protein strongly expressed in the brain. It has been shown to interact with mutant tau, which can promote neurodegeneration, but nothing is known about the physiological function of EFhd2 in the nervous system. To elucidate this question, we analyzed EFhd2(−/−)/lacZ reporter mice and showed that lacZ was strongly expressed in the cortex, the dentate gyrus, the CA1 and CA2 regions of the hippocampus, the thalamus, and the olfactory bulb. Immunohistochemistry and western blotting confirmed this pattern and revealed expression of EFhd2 during neuronal maturation. In cortical neurons, EFhd2 was detected in neurites marked by MAP2 and co-localized with pre- and post-synaptic markers. Approximately one third of EFhd2 associated with a biochemically isolated synaptosome preparation. There, EFhd2 was mostly confined to the cytosolic and plasma membrane fractions. Both synaptic endocytosis and exocytosis in primary hippocampal EFhd2(−/−) neurons were unaltered but transport of synaptophysin-GFP containing vesicles was enhanced in EFhd2(−/−) primary hippocampal neurons, and notably, EFhd2 inhibited kinesin mediated microtubule gliding. Therefore, we found that EFhd2 is a neuronal protein that interferes with kinesin-mediated transport.